Study Design. Systematic review.
Objective. To evaluate the validity of instruments that claim to detect submaximal capacity when maximal capacity is requested in patients with chronic nonspecific musculoskeletal pain.
Summary of Background Data. Several instruments have been developed to measure capacity in patients with chronic pain. The detection of submaximal capacity can have major implications for patients. The validity of these instruments has never been systematically reviewed.
Methods. A systematic literature search was performed including the following databases: Web of Knowledge (including PubMed and Cinahl), Scopus, and Cochrane. Two reviewers independently selected the articles based on the title and abstract according to the study selection criteria. Studies were included when they contained original data and when they objectified submaximal physical or functional capacity when maximal physical or functional capacity was requested. Two authors independently extracted data and rated the quality of the articles. The included studies were scored according to the subscales “Criterion Validity” and “Hypothesis Testing” of the COSMIN checklist. A Best Evidence Synthesis was performed.
Results. Seven studies were included, 5 of which used a reference standard for submaximal capacity. Three studies were of good methodological quality and validly detected submaximal capacity with specificity rates between 75% and 100%.
Conclusion. There is strong evidence that submaximal capacity can be detected in patients with chronic low back pain with a lumbar motion monitor or visual observations accompanying a functional capacity evaluation lifting test.
Level of Evidence: N/A
This systematic review evaluates the validity of instruments that claim to detect submaximal capacity when maximal capacity is requested in patients with chronic pain. Seven studies were included. Submaximal capacity can be detected in patients with chronic low back pain with a lumbar motion monitor or a functional capacity evaluation lifting test.
*Department of Research Methodology, Measurement and Data Analysis, University Twente, Enschede, the Netherlands;
†Department of Rehabilitation Medicine, Center for Rehabilitation, University Medical Center Groningen, The Netherlands;
‡Department of Work Rehabilitation, Rehaklinik Bellikon, SUVA Care, Bellikon, Switzerland;
§Department of Epidemiology, Medisch Spectrum Twente, Enschede; and
¶Condite; Disability Management, Enschede, the Netherlands.
Address correspondence and reprint requests to Suzan van der Meer, MSc, University Twente, Drienerlolaan 5, 7522 NB Enschede, the Netherlands; E-mail: email@example.com
Acknowledgment date: March 21, 2013. First revision date: May 29, 2013. Second revision date: August 22, 2013. Acceptance date: August 23, 2013.
The manuscript submitted does not contain information about medical device(s)/drug(s).
No funds were received in support of this work.
No relevant financial activities outside the submitted work.